Evidence map›Paper›PMID 32494680›Full record

ArticleScience advances2020

Cellular backpacks for macrophage immunotherapy.

C Wyatt Shields, Michael A Evans, Lily Li-Wen Wang, Neil Baugh, Siddharth Iyer, Debra Wu, Zongmin Zhao, Anusha Pusuluri, Anvay Ukidve, Daniel C Pan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 198 papers.

0numbers the graph read from it
0cells of the map it votes in
198citing papers in PubMed
20.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

198 citing papers in PubMed, 390 citations in OpenAlex.

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138 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

C Wyatt ShieldsJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0003-4138-8462
Michael A EvansJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Lily Li-Wen WangJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Neil BaughJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0002-4058-4448
Siddharth IyerJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0003-4986-4275
Debra WuJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Zongmin ZhaoJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0001-8979-844X
Anusha PusuluriJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Anvay UkidveJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0002-6757-7942
Daniel C PanJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.
Samir MitragotriJohn A. Paulson School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA.ORCID 0000-0002-2459-8305
Harvard University · US

Funding

Vascular delivery of nanocarriers by erythrocyresR01HL143806 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI MUZYKANTOV, VLADIMIR R · 2018 to 2021
$2.8M
NHLBI NIH HHS R01 HL143806
6 · The paper itself

Abstract

Adoptive cell transfers have emerged as a disruptive approach to treat disease in a manner that is more specific than using small-molecule drugs; however, unlike traditional drugs, cells are living entities that can alter their function in response to environmental cues. In the present study, we report an engineered particle referred to as a "backpack" that can robustly adhere to macrophage surfaces and regulate cellular phenotypes in vivo. Backpacks evade phagocytosis for several days and release cytokines to continuously guide the polarization of macrophages toward antitumor phenotypes. We demonstrate that these antitumor phenotypes are durable, even in the strongly immunosuppressive environment of a murine breast cancer model. Conserved phenotypes led to reduced metastatic burdens and slowed tumor growths compared with those of mice treated with an equal dose of macrophages with free cytokine. Overall, these studies highlight a new pathway to control and maintain phenotypes of adoptive cellular immunotherapies.

Indexed as

ImmunotherapyMacrophagesAnimalsCytokinesImmunologic FactorsImmunotherapy, AdoptiveMicePhagocytosisCytokinesImmunologic Factors

Identifiers

PMID32494680
PMCPMC7190308
OpenAlexW3021413923

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.